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A New Method for the Oxybromination of Aromatic Compounds with Copper(II)bromide and Potassium Dichromate

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TLDR
In this paper, a new and mild method for oxybromination of aromatic compounds with CuBr 2 and K 2 Cr 2 O 7 in HOAC was reported, which is a milder version of the traditional method.
Abstract
A new and mild method for oxybromination of aromatic compounds with CuBr 2 and K 2 Cr 2 O 7 in HOAC is reported.

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Oxidative bromination reaction using Cu2+-perfluorophthalocyanine-immobilized silica gel catalyst under mild reaction conditions

TL;DR: In this article, a simplified route has been applied for the grafting of copper(II) perfluorophthalocyanine complex onto functionalized silica gel, and the resulting organic-inorganic hybrid material is used as an efficient and recyclable catalyst for the regioselective oxidative bromination of various aromatic substrates using KBr/H2O2 as the reagents, affording high yields under mild conditions.
Journal ArticleDOI

Cross-Dehydrogenative-Coupling of Alkoxybenzenes with Toluenes: Copper(II) Halide Mediated Tandem Halo/Benzylation of Arenes.

TL;DR: Preliminary mechanistic studies suggest that the in situ production of haloarenes followed by a copper-mediated coupling of a benzylic radical is operational.
Journal ArticleDOI

A New Method for the Oxybromination of Aromatic Compounds with Copper(II)bromide and Potassium Dichromate.

TL;DR: In this paper, a new and mild method for oxybromination of aromatic compounds with CuBr 2 and K 2 Cr 2 O 7 in HOAC was reported, which is a milder version of the traditional method.
References
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Journal ArticleDOI

An efficient and regioselective oxybromination of aromatic compounds using potassium bromide and oxone

TL;DR: In this paper, a simple and regioselective method for oxybromination of aromatics is reported. And the electrophilic substitution of bromine generated in situ from potassium bromide using oxone® as an oxidant is described.
Journal ArticleDOI

Electrophilic halogenation of aromatics and heteroaromatics with N-halosuccinimides in a solid/liquid system using an H+ ion exchanger or ultrasonic irradiation

TL;DR: In this paper, the halogenation of thiophene, its methyl and halo derivatives as well as activated arenes (mesitylene, 1,3-dimethoxybenzene, 2,3dimethylanisole) in a two-phase hexane/solid N-halosuccinimide system is catalysed by the strongly acidic sulfonated resin Amberlyst® 15.
Journal ArticleDOI

Liquid phase bromination of aromatics over zeolite H-beta catalyst

TL;DR: In this article, the authors investigated the performance of N -bromosuccinimide (NBS) and liquid Br 2 as brominating agents in the liquid phase bromination of chlorobenzene, toluene and xylenes.
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